BACKGROUND OF THE INVENTIONField of the Invention
The present invention relates to a magnetic stimulus type urinary incontinence treatment apparatus for magnetically treating a patient for urinary incontinence by supplying pulse current and thereby generating flux for generating eddy current in a physiological body.
As a urinary incontinence treatment, an electrical stimulus treatment for stress incontinence, urge incontinence and the like by fitting a stimulus electrode to a physiological body and supplying electrical pulses thereto has been well known in addition to a medical treatment and the like. In case of the electrical stimulus treatment, a plug-shaped electrode having a diameter of 2 cm and a length of 4 cm for a vagina or double enveloping electrode having the same dimensions for an anus connected to a pulse wave generator is inserted into the vagina or anus, and pulse current of a repeated frequency of several Hz to several tens Hz, a peak current of 1 to 100 mA and a pulse width of 100 μs to 1 ms is applied directly from the body surface. By so doing, pelvic floor muscle is stimulated and trained by the pulse current applied from the body surface and the weaken muscle is reinforced to thereby strengthen the force for tightening a urethra. Thus, it is effective in the treatment for stress incontinence.
As for urge incontinence caused by the involuntary contraction of a urinary bladder, pudendal nerves or their branches formed from the second to fourth sacral nerves of lunbosacral plexus are stimulated to thereby reflexively prevent the involuntary contraction of the urinary bladder, whereby urinary incontinence can be prevented.
However, the above-stated electrical stimulus treatment using a plug-type electrode requires inserting the electrode into the vagina or anus every time the treatment is conducted. Due to this, there occur problems such as a patient refuses treatment or refuses to continue treatment. Furthermore, if stimulus current is increased so as to obtain a prompt effect in a short period time, there is a possibility that this gives rise to a pain or, what is worse, a burn.
In these circumstances, the present applicant proposed a urinary incontinence treatment apparatus wherein a magnetic stimulus coil for generating repeated pulse-like flux provided at a coil installation tool installed in a room are fitted to regions from the patient's waist to crural region and the flux applied into the body allows eddy current to stimulate pelvic floor muscle, pudendal nerves and the like, as disclosed in the U.S. patent application Ser. No. 08,800,709.
This has made it possible to realize a urinary incontinence treatment apparatus capable of treating a patient for a disease without giving pain to the patient in a non-invasion manner while the patient has his or her clothes on. Meanwhile, in such a treatment, it is necessary to give consideration to electrical power efficiency and, in some cases, to provide a forced cooling system for forcedly cooling a magnetic stimulus coil to supply high current to the coil. Moreover, it is preferable that regions such as a womb, an ovary, a urinary bladder, testicles, which are not directly relevant to the treatment are not stimulated.
SUMMARY OF THE INVENTIONIn view of the above respects, it is therefore an object of the present invention to provide a magnetic stimulus type urinary incontinence treatment coil apparatus capable of stimulating regions effective for the urinary incontinence treatment in a concentrated manner.
To obtain the object, according to the present invention, the magnetic stimulus type urinary incontinence treatment coil apparatus generates flux for generating eddy current in a physiological body by comprising a foil having at least an upper surface curved in a concave manner in a longitudinal direction such that the coil is wound along and fitted to at least part of a region from an upper face region of a female patient's urethra opening to a rear face of her anus; and a support for supporting the coil to a position at which the coil is fitted to the patient.
Due to the upper surface having a corresponding concave curved shape, the coil is closely attached to or comes in at least close contact with at least part of the region from an upper face region positioned in front of the urethra opening to a rear face region positioned in the back of the anus. By so doing, eddy current due to flux is generated at a position outside of the patient's body close to a magnetic stimulus target region while the front and rear coil portions approach each other from the same plane in the direction in which they face each other.
According to the present invention, the coil is fitted to be closely attached to or comes in close contact with a fitting target position. Therefore, flux is generated while oriented to the stimulus target region and the region can be stimulated with high eddy current generated by strong magnetic field on the coil surface. The region is effectively stimulated while avoiding stimulating irrelevant regions. Treatment without the need to forcedly cooling the coil is also possible.
In addition, to further narrow the flux generation limit to a desired magnetic stimulus target region, the apparatus according to the present invention is characterized by comprising a coil wound around a magnetic core and a support for supporting the magnetic core to a position at which the coil is fitted to the patient and in that the magnetic core is formed such that the front and rear end faces of the coil are fitted to at least pat of a region from a front face region of a female patient's urethra opening to a rear face region of her anus. The end faces of the magnetic core are fitted to be closely attached to or at least come in close contact with at least part of a region from the front face region of the urethra opening to the rear face region of the anus. By so doing, eddy current passing both pelvic floor muscle and pudendal nerves distributing below the pelvic floor muscle or passing only the pudendal nerves is generated by the flux produced in a concentrated manner in the vicinity of end faces serving as magnetic poles positioned outside the patient's body close to the magnetic stimulus target region.
Moreover, according to the present invention, for purposes of allowing positions of front and rear coils to be adjustable in a longitudinal direction independently of each other, a pair of front and rear rotating plates having inner end portions adjacent to each other are rotatably supported by a tip end portion of a support such that positions of the rotating plates are adjusted in a longitudinal direction, respectively, and a pair of front and rear coils wound around surfaces of the rotating plates are provided at the rotating plates, respectively. The upper surface part of the rear coil of the coils of the front rotating plate and an upper surface part of the front coil of the coils of the rear rotating plate are positioned such that the upper surface parts are fitted to at least regions from a front face region of a urethra opening at rotating adjusted positions, and the pair of front and rear coils are supplied with current in directions opposite to each other. While the patient is seated or standing, the coils provided at the pair of rotating plates, respectively are fitted to be closely attached to or at least come in close contact with at least part of a region from the front end region of the urethra opening to the rear face region of the anus by adjusting the pair of rotating plates in the longitudinal direction, independently of each other.
BRIEF DESCRIPTION OF THE DRAWINGSFIG. 1 shows an air-core type coil apparatus in an embodiment according to the present invention. FIG. 1A is a cross-sectional view of the important parts of the apparatus and FIG. 1B is a back view thereof.
FIG. 2 shows a modification of the coil apparatus shown in FIG.1. FIG. 2A is a front view and FIG. 2B is a side view of the apparatus.
FIG. 3 is a perspective view of a urinary incontinence treatment apparatus employing the coil of FIG.1.
FIG. 4 shows a feeder system for the apparatus of FIG.3. FIG. 4A shows a circuit arrangement of the feeder system and FIG. 4B shows output pulses of the circuit of FIG.4A.
FIG. 5 is a cross-sectional view of the important parts of an air-core type coil apparatus in another embodiment according to the present invention.
FIG. 6 is a perspective view showing a support of the coil shown in FIG.5.
FIG. 7 is a cross-sectional view and a plan view showing the typical shape of the air-core type coil according to the present invention.
FIG. 8 is a cross-sectional view of the important parts of the coil apparatus having a magnetic core installed at the air-core part of the air-core type coil of FIG.1.
FIG. 9 is a cross-sectional view of the important parts of a coil having with one magnetic core in an embodiment according to the preset invention.
FIG. 10 is a perspective view showing part of a support of the coil shown in FIG.9.
FIG. 11 shows a coil fitting type coil apparatus in another embodiment according to the preset invention. FIG. 11A is a cross-sectional view of the apparatus with one coil and FIG. 11B is a cross-sectional view of the apparatus with two coils. FIG. 11C is a cross-sectional view of a coil which is a modified version of the coil of FIG. 11A or FIG.11B. FIG. 11D is a front view of the coil shown in FIG.11C.
FIG. 12 is a perspective view of a support in another embodiment according to the present invention.
FIG. 13 is a cross-sectional view showing the important parts of the rotatable plate type coil apparatus.
FIG. 14 shows the coil apparatus of FIG.13. FIG. 14A is a perspective view of the apparatus and FIG. 14B is a cross-sectional view showing part of the apparatus.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTSDescription will be given to a magnetic stimulus type urinary incontinence treatment coil apparatus in an embodiment according to the present invention, with reference to FIGS. 1 through 4. In FIG. 3, reference numeral9 denotes a urinary incontinence treatment apparatus. The apparatus comprises afeeder system2 in the back of a chair serving as a support of the apparatus, and acoil10 provided on aseat1a.
As shown in FIGS. 1A and 1B, the coil consists of three layers formed by rectangularly coiling arectangular conductor11 having an insulating material coated film three times along a patient's fitting target region while anair core part11ais formed at the center. These three layers are connected to one another in parallel and also connected to thefeeder system2. The upper surface is formed to be curved in a concave manner in the longitudinal direction such that afront coil part10awhich is in front of theair core part11ais fitted along a region of aurethra opening3 and arear coil part10bis fitted along a region of an anus4. According to the plan view, the coil has a longitudinal width of about 200 mm and a lateral width slightly smaller than the standard gap between joints of both femoral regions to about 100 mm, and the air-core part has a longitudinal width of about 80 mm, a lateral width of about 10 mm and a radius of curvature of about 100 mm. Thecoil10 has respective layers connected to one another and is embedded into theseat part1aserving as a cushion while thecoil10 remains slightly protruding therefrom such that thecoil10 is securely and closely attached to the fitting target region.
As shown in FIGS. 2A and 2B, the central portion of thecoil10 in the lateral direction is preferably protuberant in a corrugated manner to ensure closely fitting the coil to the target region. It is possible to protrude thecoil10 higher with smaller width instead of the corrugate shape.
FIG. 4A shows a circuit arrangement of thefeeder system2. Thefeeder system2 consists of aDC power supply15 capable of adjusting voltage in a range between 100 V to 2 kV, a capacitor C1 of about 300 μF to be charged by the DC power supply, athyristor16 for applying the charging voltage to thecoil10 through a protective resistor R1, a thyristor16afor absorbing reverse voltage in a switch-off state and aswitching control circuit17 for on-controlling, that is, ignition-controlling these thyristors through atransformer16b.The repeated frequency of the switchingcontrol circuit17 can be adjusted in a range between 1 Hz and 100 Hz. The winding structure of thecoil10, the voltage of theDC power supply15 and the capacity of the capacitor C1 allow entire current pulses of about 100 μs of thecoil10 to generate flux of a flux density of a peak value of about 0.01 to 3 teslas at a maximum of about 3000 A by adjusting voltage.
As shown in the upper part of FIG. 4B, at the switchingcontrol circuit17, not only a single pulse but also double pulses of about 100 μs as stated above can be employed so as not to give pain to the patient as a result of making a pulse wider. Depending on the state and symptom of the stimulus target region of the patient, various pulse stimulus modes can be selected such as a plurality of continuous pulses, bipolar double pulses shown in the lower part of FIG.4B. The pulse width is not limited to 100 μs, but can be set to about 1 μs to 2 ms depending on the state and symptom of the stimulus target region as in the case of the conventional electrical stimulus treatment.
At the time of treatment, as shown in FIG. 1, the patient sits down on theseat part1awith his or her clothes on. Thefront coil part10aslightly protruding at its central portion is fitted to theurethra opening3 and therear coil part10bis fitted to a region of the anus4. If current is applied in this state, eddy current due to flux is generated at a position outside the patient's body close to magnetic stimulus target regions, that is, the pelvic floor muscle B1 and pudendal nerves B2 distributing into the lower portion of the pelvic floor muscle B1 among the pudendal nerves B2 while thefront coil part10aand therear coil part10b, respectively approach each other from the same plane and closely are attached to regions of theurethra opening3 and anus4. As a result, the pelvic floor muscle B1, external urethral spincter directly surrounding the urethra, the pudendal nerves B2 and the like are stimulated by ebby current, thus making it possible to effectively conducting treatment for both the urge incontinence and the stress incontinence. The pelvic floor muscle B1 and the pudendal nerves B2 are effectively stimulated without unnecessary gaps provided while avoiding stimulating regions such as aurinary bladder6, awomb7, an ovary, testicles and the like which are irrelevant to the treatment. Since the hip region is supported at theseat part1a, the patient feels it comfortable to sit down on theseat part1aand does not feel tired. Normally, it is enough to apply electric current to such an extent that no forced cooling is required. If needed, however, it may be set to a maximum of about 200 W on condition of cooling the coil.
FIGS. 5 and 6 show a small size coil apparatus of, again, air core type. Acoil20 is formed to be a closed shape having a longitudinal width of 30 mm and a lateral width of 20 mm according to a plan view. Thecoil20 also consists ofconductors21 insulated from each other on both ends facing each other. The air-core part of thecoil20 is fitted into ahead part22aof acoil holding member22 made of synthetic resin. Upper surfaces of theconductors21 and theheat part22aare molded to have convex surfaces corresponding to theurethra3 and its surrounding surface regions. Thecoil holding member22 is slightly protruded from aseat part23 of bicycle saddle shape installed on the tip end portion of astand24 such that the upper surface of thecoil20 can be securely and closely attached to the surface regions around theurethra opening3. In this case, the pudendal nerves B2 are mainly stimulated, which is effective against urge incontinence.
FIG. 7 shows a typical shape of coils including the above-stated coil according to the present invention. According to the plan view, the longitudinal width L1 of the outer dimension is 30 to 300 mm and the lateral width W1 is 20 to 120 mm. The longitudinal width L2 of the air core part is 20 to 160 mm and the lateral width W2 thereof is 10 to 40 mm. The radius of curvature R on the upper surface of the coil is 90 to 150 mm. A female patient of large build has a longitudinal width L1 of about 300 mm from an upper face region in front of the urethra opening to a rear face region in the back of the anus, and has a lateral width W1 of a maximum of about 120 mm corresponding to the gap between joints of the both femoral regions. The larger the shape, that is, the larger the inner dimension of the air-core part is, the deeper from the body surface the eddy current can be generated and the shape or inner dimension is specified by a width of a conductor with respect to its outer dimension. By using such a coil, the highest eddy current is flown though a region right on the coiled conductor. However, the upper surface is not necessarily completely arc shaped. It can precisely correspond to the shape of the fitting target region and, in some cases, may be slightly curved in the lateral direction. The curved shape of the coil can be provided by molding the surface of the conductor, or by coiling a plurality of conductors along curved surfaces. Furthermore, the shape of the coil is not limited to rectangular. It may be circular, ellipsoidal and the like depending on the stimulus target region.
FIG. 8 shows a coil apparatus wherein amagnetic core29, such as a ferrite core, having good frequency characteristics and low loss is fitted into the air-core part11aof thecoil10 shown in FIG.1. In this case, by shallowly concentrating a flux generation region into a central portion, the pudendal nerves B2 are mainly stimulated in a concentrated manner while the flux hardly arrives at the pelvic floor muscle B1. This is especially effective in the treatment for urge incontinence and it can greatly prevent regions irrelevant to the treatment from being stimulated.
FIG. 9 shows a magnetic core fitting type coil apparatus for fitting a magnetic core to a patient. A front end face35aserving as one magnetic pole of a U-shapedmagnetic core35 around which acoil30 is wound is located at a slightly upper position than a rear end face35bserving as the other magnetic pole thereof and upper surfaces thereof are formed to be concave curved such that the front end face35ais fitted to a front face region of the female patient'surethra opening3 and the rear end face35bis fitted to a rear face region of the patient's clitoris. Themagnetic core35 is fitted into aconcave portion37aof a holdingmember37 made of synthetic resin and having an upper surface slightly concave-curved. As shown in FIG. 10, the holdingmember37 is installed on theseat part1asuch that the end faces35aand35bare slightly protruded from the above-mentionedseat part1a, and the lower end portion of thecoil30 is exposed to be air-cooled. By so doing, the arch like flux can be generated between the end faces35aand35bin a convergent manner to thereby stimulate both the pelvic floor muscle B1 and the pudendal nerves B2. Since the flux can be generated in an effectively convergent manner, power consumption can be greatly reduced.
FIG. 11A shows a coil apparatus of, again, magnetic core fitting type. A front end face45aof a U-shapedmagnetic core45 around which acoil40 is wound, is located at a slightly upper position than a rear end face45band upper surfaces thereof are formed to be concave-curved such that the front end face45ais fitted to a region of the female patient'surethra opening3 and the rear end face45bis fitted to a region of aclitoris5. The portion between the end faces45aand45bis molded and the surfaces thereof are formed on corresponding curved surface, respectively. Themagnetic core45 is embedded into aseat part42 of a chair or stand having a central portion in the longitudinal direction curved to be of corresponding concave shape. In this case, the end faces45aand45bserving as magnetic poles are fitted to come in close contact with a fitting target region. Since the distance between the end faces45aand45bis short, the flux does hardly reach the pelvic floor muscle B1 and mainly stimulates the pudendal nerves B2.
In FIG. 11B, thecoil40 includes twocoil parts40aand40b. Thecoil parts40aand40bare wound in the vicinity of the end faces45aand45bof the U-shapedmagnetic core45 positioned in the vicinity of the female patient'surethra opening3 and theclitoris5, respectively and current is supplied to thecoil parts40aand40b, respectively such that the flux of thecoil parts40aand40bflows through themagnetic core45 in the same direction.
As shown in FIG. 11C, thecoil40 consists of aconductor46 coiled once to be U-shaped. Thecoil40 comprises afront coil part40csurrounding vicinity of theurethra opening3 by forming an air-core part48 and arear coil part40dsurrounding the vicinity of the anus4 by forming an air-core part48. The central portion of the conductor of these coil parts are protuberant in the lateral direction as shown in FIG.11D. It is possible to install a common U-shaped magnetic core at the air-core part48 of theconductor46. Alternatively, thecoil40 can be continuously wound by one conductive line.
FIG. 12 shows a stand type coil support. Apipe51 of the support slidably supports a rod having acoil50 with an air core or a magnetic core installed on a tip end portion thereof. The position of thecoil50 can be locked to a position slidably adjusted by athumbscrew52. The support enables thecoil50 to be fitted to a patient who remain standing while adjusting the position of thecoil50 as required.
FIGS. 13 and 14 show a rotation type coil apparatus. Complementary-shape protrusion parts62 and62aon inner end portions of a pair ofrotating plates61 and61ainto which coils60 and60aare embedded, respectively, are rotatably supported by arotation axis64 of astand65. Athumbscrew66 is engaged with therotation axis64 and the rotating operation allows aflange part64aon the opposite end of therotation axis64 to be secured to thestand65 and the adjusted position to be locked. Moreover, thestand65 is provided with astopper66 for supporting therotating plates61 and61ain the horizontal direction. The lateral widths of therotating plates61 and61aare set in accordance with the gap between the joints of both femoral regions to, for example, 100 mm.
Thecoils60 and60aare wound around surfaces of the correspondingrotating plates61 and61asuch that air core parts are formed at central portions, respectively. The coilupper surface portion60bwhich is in the rear of the air-core part of thecoil60 on the frontside rotating plate61 and the coilupper surface part60cwhich is in front of the air core part of thecoil60aof the rearside rotating plate61aare positioned such that the coilupper surface part60bis fitted to a region of a female patient'surethra opening3 and the coilupper surface part60cis fitted to a region of the patient'sclitoris5. Thecoils60 and60aare connected such that they are supplied with current flowing opposite directions.
By so doing, the rotation position is adjusted in accordance with the patient's form and the coilupper surface part60bis fitted to theurethra opening3 and the coilupper surface part60cis fitted to theclitoris5, thereby stimulating mainly the pudendal nerves B2. It is noted here that if the coilupper surface part60cis deformed to be positioned in a rear face region of theclitoris5, a flux generation region becomes wider and the pelvic floor muscle can be simultaneously stimulated.
It is also possible to install therotating plates61 and61aon the tip end portion of the stand as shown in FIG.12 and to provide a coil apparatus capable of treating a patient while the patient remains standing. In that case, the lateral widths of therotating plates61 and61aare set to be slightly smaller than that of the standard gap between the joints of femoral regions. In addition, the rotatingplates61 and61aare friction-engaged with the rotation axis and held at appropriate adjusted positions so that the structure of the side of the thumbscrew and the like may not be a hindrance to the apparatus.